Chemotherapy With or Without Dalteparin in Treating Patients With Metastatic Pancreatic Cancer (PAM07)

GERCOR - Multidisciplinary Oncology Cooperative Group

Status and phase: Terminated; Phase 3

Conditions: Thromboembolism; Chemotherapeutic Agent Toxicity; Pancreatic Cancer

Treatments: Drug: Chemotherapy at the investigator's discretion; Drug: daltéparine

Study type: Interventional

Funder types: Other

Identifiers

NCT00662688

EUDRACT 2007-002115-59

EU-20837

GERCOR-PAM07-D07-2

CDR0000593019

PFIZER-GERCOR-PAM07-D07-2

Details and patient eligibility

About

RATIONALE: Drugs used in chemotherapy, such as gemcitabine and capecitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Anticoagulants, such as dalteparin, may help prevent blood clots from forming in patients being treated with chemotherapy. It is not yet known whether gemcitabine is more effective when given alone or together with dalteparin and/or capecitabine in treating patients with pancreatic cancer.

PURPOSE: This randomized phase III trial is studying whether dalteparin prevents blood clots in patients with pancreatic cancer receiving treatment with different combinations of gemcitabine and capecitabine.

Full description

OBJECTIVES:

Primary

• To demonstrate that preventive anticoagulation with dalteparin reduces the number of thromboembolic events.
• To determine the number of thromboembolic events occurring with preventive anticoagulation.

Secondary

• To determine survival without thrombotic event.
• To determine progression-free and overall survival.
• To determine time to response of tumor.
• To assess tolerance of these regimens.

OUTLINE: This is a multicenter study. Patients are stratified according to participating center and WHO performance status (0-1 vs 2). Patients are randomized to 1 of 4 treatment arms.

• Arm A: Patients receive chemotherapy at investigator's discretion
• Arm B Patients receive chemotherapy at investigator's discretion and dalteparin In all arms, treatment repeats in the absence of disease progression or unacceptable toxicity.

Blood and plasma samples are obtained at baseline and periodically during study. Blood is examined for biomarkers, resistance to activated protein C, and mutations (Leiden V factor, mutation G20210A, and the factor II gene). Thrombin generation and factors VIIa and VIII are assessed in plasma.

After completion of study therapy, patients are followed periodically.

Enrollment: 42 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed adenocarcinoma of the pancreas

  • Metastatic disease
  • Not amenable to treatment
  • No localized or locally advanced disease

• Measurable disease (metastatic or primary tumor) defined as ≥ 2 cm by CT scan or ≥ 1 cm by spiral CT scan or MRI

• No progressive thrombo-embolic disease

• No adenocarcinoma of the biliary tract or ampulla of Vater

• No known CNS metastases

PATIENT CHARACTERISTICS:

• WHO performance status 0-2

• Life expectancy > 12 weeks

• ANC ≥ 1,500/mm^3

• Platelet count ≥ 100,000/mm^3

• Hemoglobin ≥ 9 g/dL

• Alkaline phosphatase < 5 times normal

• Bilirubin < 1.5 times normal

• Creatinine < 1.5 times normal

• Creatinine clearance < 30 mL/min

• Pain controlled or stabilized via analgesic therapy

• Affiliation with social security system

• Not pregnant or nursing

• No controlled or uncontrolled jaundice

• No contraindication to study drugs

• No cardiovascular accident (myocardial infarction, cerebral vascular accident) within the past 6 months

• No serious cardiac and/or respiratory disease

• No other cancer in the past 5 years except the following cancers, provided they have been completely resected:

  • Skin cancer
  • Localized melanoma
  • Carcinoma in situ of the cervix

• No history of thrombophilia

• No history of heparin-induced thrombocytopenia

• No uncontrolled or persistent hypercalcemia

• No psychological, familial, social, and/or geographical condition that precludes participation in the study

PRIOR CONCURRENT THERAPY:

• No prior hematologic therapy for metastatic disease
• No prior abdominal radiotherapy
• No concurrent corticosteroids as anti-emetic therapy
• No other concurrent anticoagulation

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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42 participants in 2 patient groups

chemotherapy

Active Comparator group

Description:

chemotherapy at investigator's discretion

Treatment:

Drug: Chemotherapy at the investigator's discretion

dalteparin

Experimental group

Description:

dalteparin: 5000 UI sub-cutaneous injection, from Day 1 to Day 28.

Treatment:

Drug: Chemotherapy at the investigator's discretion

Drug: daltéparine